8-Hydroxy-9,15-dihydro-7 H-diindeno [ Z , l -b ; 2', l'-g] fluorene, a derivative of a new mono-angular diindenofluorene system, has been synthesised in 6 steps (overall yield 420/,) starting from 9-oxo-fluorene-l-carbaltlehyde and acetophenone. The corresponding hydrocarbon could not be obtained by
Synthèses dans la série des bis-indéno-fluorènes, VIII. Méthyl-6-dihydro-9,15-7H-bis-indéno[2.1-b;2′.1′-g]fluorène
✍ Scribed by Louis Chardonnens; Thomas Stauner
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- German
- Weight
- 298 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Starting from 5‐benzoyl‐2,4‐dibromobenzoic acid and 3‐methyl‐fluorene, the 6‐methyl‐9,15‐dihydro‐7H‐diindeno[2.1‐b; 2′,1′‐g]fluorene, a derivative of a mono‐angular diindenofluorene has been synthesized in 5 steps (overall yield 1,5%).
📜 SIMILAR VOLUMES
Ill] AECKERT & F.SEIDEL, J. prakt. Chem. [2] 102, 358 (1921).
## Abstract Starting from 3, 4‐dimethylfluorene the title compound, 5, 6‐dimethyl‐7, 12‐dihydro‐indeno[1,2‐a]fluorene (IV), is synthesized in four steps (overall yield 9%). The same hydrocarbon is also obtained in four steps starting from the phthalaconecarboxylic acid of __Gabriel__. This corrobor